Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Ford Mustang Mach-E Power Loss Problems Results in Recall of 34,762 Vehicles With Extended-Range BatteriesThe latest Ford Mustang Mach-E recall comes after the NHTSA determined that previously recalled vehicles equipped with extended range batteries did not receive satisfactory repair, and may still suddenly lose power while driving. October 23, 2023 Katherine McDaniel Add Your CommentsNearly 35,000 Ford Mustang Mach-E vehicles that were previously recalled due to battery failures are being recalled again, due to defects that may cause unexpected loss of motive power, even after prior recall repairs were completed.The National Highway Traffic Safety Administration (NHTSA) announced the Ford Mustang Mach-E recall on October 17, after investigating more than one hundred consumer complaints involving vehicles losing power after receiving Fordโs recall remedy.The vehicles were subject to a recall in June 2022, after it was discovered that the high voltage battery contactors could overheat, causing an immediate loss of vehicle power, increasing the risk of an auto accident.Ford provided affected vehicle owners with a Secondary On-Board Diagnostic Control Module (SOBDMC) software update, and a Battery Energy Control Module (BECM) software update, to prevent further damage by monitoring the temperature and reducing battery power. The automaker also issued a technical service bulletin to replace the High Voltage Battery Junction Box (HVBJB) to remedy the issue.However, the NHTSA has received multiple reports of repaired vehicles continuing to lose motive power after receiving the software updates and replacement HVBJB, which prompted an investigation into the recall remedy.Ford Mustang Mach-E Recall Repair InvestigationFord initially became aware of the power failure problems and issued a recall in June 2022, affecting approximately 48,924 model year 2021 through 2022 vehicles manufactured from May 27, 2020 until May 24, 2022. The recall followed hundreds of warranty claims involving overheated high voltage battery contactors, which prevented the parts from properly closing or welded them shut.The NHTSA warned that the battery issues could result in an immediate loss of vehicle power, which could lead to the driver losing control of the vehicle and getting into an accident.To rectify the issue, Ford provided diagnostic and battery energy control module software updates intended to monitor the contactorโs temperature, identify overheating, and reduce battery power to avoid further contactor damage. The software updates were introduced into the production of new Mustang Mach-E vehicles beginning on May 25, 2022. Months later, the automaker released a technical service bulletin to replace the battery junction box of the recalled vehicles.Following the recall repairs, federal safety officials launched a Ford Mustang Mach-E recall repair investigation on August 17 to determine whether the repairs were adequate, after the agency received at least 12 reports from owners who continued to experience battery failures and loss of driving power after receiving the software updates and replacement parts.The investigation involved approximately 64,727 model year 2021 through 2022 Ford Mustang Mach-E vehicles. It included vehicles subject to the recall, as well as vehicles produced with the updated software beginning on May 25, 2022, following the recall.According to the NHTSA investigation, the vehicleโs high voltage battery main contactors were overheating and deforming due to the direct current (DC) fast charging combined with repeated high acceleration events, which caused the battery to fail and resulted in loss of vehicle power.Officials determined that while Fordโs recall remedy addressed the loss of motive power in vehicles equipped with standard range batteries, it did not rectify the issue for certain vehicles equipped with extended range batteries, which have a much higher probability of sustaining damage to the battery contactors, as they require more electrical power.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONFord Mustang Mach-E RecallThe new Ford Mustang Mach-E recall impacts approximately 34,762 model year 2021 through 2022 Mustang Mach-E vehicles equipped with extended range batteries that were produced between May 27, 2020 and May 24, 2022.Standard range battery vehicles were not included in the recall, as the variants requires much less power and have a lesser chance of sustaining damage to the contactor.While no accidents or injuries have been reported in relation to the recalls, Ford has become aware of at least 107 consumer complaints involving vehicles losing power after the high voltage contactors overheated, of which 100 of the incidents involved a higher powered GT or extended range battery vehicle.Ford expects to begin notifying owners of the recall by mail beginning on October 30, with instructions on how to receive free replacement of their High Voltage Battery Junction Box (HVBJB) by a licensed dealer.For more information, owners may contact Ford customer service by phone at 1-866-436-7332 and reference recall number 23S56. They may also contact the NHTSAโs Vehicle Safety Hotline by phone at 1-888-327-4236 (TTY 1-800-424-9153), or visit their website at https://www.nhtsa.gov. Tags: Auto Accident, Auto Recall, Battery Recall, Electric Car, FordMore Lawsuit Stories $53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula April 10, 2026 Nurse Assist Saline Solution Lawsuit Alleges Contamination Caused Severe Infection April 10, 2026 Oster Countertop Oven Lawsuit Claims Recalled Device Caused Third Degree Burns April 10, 2026 0 Comments EmailThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES $53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula (Posted: yesterday)A jury has awarded $53 million to four mothers who say their children suffered life-altering NEC injuries from being fed Similac infant formula shortly after being born preterm.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITEnfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects (03/12/2026)High Levels of Heavy Metals Found in More Than 25 Additional Infant Formulas: Report (03/09/2026)Trial Over Similac Necrotizing Enterocolitis Injuries Underway in Chicago (03/06/2026) Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (Posted: 2 days ago)AngioDynamics faces a Vortex port lawsuit from a woman who says the device only lasted a month before causing an infection and dangerous blood clots in her neck.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Infection Lawsuit Claims SmartPort Defects Caused Sepsis, Pulmonary Embolism (03/23/2026)Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death (03/13/2026)Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (03/06/2026) Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (Posted: 3 days ago)A new claim against Boston Scientific joins a growing number of spinal cord stimulator lawsuits alleging the systems have failed to relieve pain and instead worsened symptoms for many individuals.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMedtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)
$53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula April 10, 2026
$53M Awarded to Families of Babies Who Developed NEC From Similac Special Care Formula (Posted: yesterday)A jury has awarded $53 million to four mothers who say their children suffered life-altering NEC injuries from being fed Similac infant formula shortly after being born preterm.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITEnfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects (03/12/2026)High Levels of Heavy Metals Found in More Than 25 Additional Infant Formulas: Report (03/09/2026)Trial Over Similac Necrotizing Enterocolitis Injuries Underway in Chicago (03/06/2026)
Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (Posted: 2 days ago)AngioDynamics faces a Vortex port lawsuit from a woman who says the device only lasted a month before causing an infection and dangerous blood clots in her neck.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Infection Lawsuit Claims SmartPort Defects Caused Sepsis, Pulmonary Embolism (03/23/2026)Chemotherapy Injection Port Lawsuit Blames AngioDynamics SmartPort for Wrongful Death (03/13/2026)Port Catheter Lawyers Outline Process for Selecting Bellwether Lawsuits in AngioDynamics MDL (03/06/2026)
Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (Posted: 3 days ago)A new claim against Boston Scientific joins a growing number of spinal cord stimulator lawsuits alleging the systems have failed to relieve pain and instead worsened symptoms for many individuals.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMedtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)